(S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one

Base Information

Chemical Name:(S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one
CAS No.:1279062-61-1
Molecular Formula:C₂₃H₃₀N₂O₄
Molecular Weight:398.502
Hs Code.:

Synonyms:(S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one

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Chemical Property of (S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one

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Technology Process of (S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one

There total 4 articles about (S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1058159-94-6
toluene-4-sulfonic acid (S)-7-oxo-2,3-dihydro-7H-oxazolo[3,2-a]pyrimidin-2-ylmethyl ester

: 4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenol

: 1279062-61-1
(S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one

Guidance literature:: 4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenol; With caesium carbonate; In tetrahydrofuran; acetonitrile; at 20 ℃;

toluene-4-sulfonic acid (S)-7-oxo-2,3-dihydro-7H-oxazolo[3,2-a]pyrimidin-2-ylmethyl ester; In tetrahydrofuran; acetonitrile; at 20 ℃; for 336h;

Reference yield:

: 78-59-1
3,5,5-Trimethylcyclohex-2-en-1-one

: 1279062-61-1
(S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: N,N,N,N,-tetramethylethylenediamine / copper(l) iodide / diethyl ether; tetrahydrofuran / 0.25 h / 0 °C

1.2: 16.5 h / 0 - 20 °C

2.1: tetrahydrofuran / 15 h / 20 °C / Cooling with ice

3.1: toluene-4-sulfonic acid / methanol / 1 h / 20 °C

4.1: caesium carbonate / acetonitrile; tetrahydrofuran / 20 °C

4.2: 336 h / 20 °C

With N,N,N,N,-tetramethylethylenediamine; caesium carbonate; toluene-4-sulfonic acid; copper(l) iodide; In tetrahydrofuran; methanol; diethyl ether; acetonitrile;

Reference yield:

: 36637-44-2
(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)magnesium bromide

: 1279062-61-1
(S)-2-[4-(3-hydroxy-1,3,5,5-tetramethyl-cyclohexyl)-phenoxymethyl]-2,3-dihydro-oxazolo[3,2-a]pyrimidine-7-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: N,N,N,N,-tetramethylethylenediamine / copper(l) iodide / diethyl ether; tetrahydrofuran / 0.25 h / 0 °C

1.2: 16.5 h / 0 - 20 °C

2.1: tetrahydrofuran / 15 h / 20 °C / Cooling with ice

3.1: toluene-4-sulfonic acid / methanol / 1 h / 20 °C

4.1: caesium carbonate / acetonitrile; tetrahydrofuran / 20 °C

4.2: 336 h / 20 °C

With N,N,N,N,-tetramethylethylenediamine; caesium carbonate; toluene-4-sulfonic acid; copper(l) iodide; In tetrahydrofuran; methanol; diethyl ether; acetonitrile;